A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506207



Internal ID20879484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20029041..20075155hg38UCSC Ensembl
chr17:19932354..19978468hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3846115
hg1946115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034850
Samples
Known GenesSPECC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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